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The 5,6-diphenylmorpholinone 3a has been used both as a nucleophilic glycine equivalent and precursor for in situ prepartion of the electrophilic 3b (a)
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The 5,6-diphenylmorpholinone 3a has been used both as a nucleophilic glycine equivalent and precursor for in situ prepartion of the electrophilic 3b. (a) Williams, R. M. Aldrichim. Acta 1992, 25, 11.
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3b and 3c have been converted to arylglycines by Mannich reaction with arenes
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3b,c were made in 5-6 steps from phenylglycine, and 3a from benzoin
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31
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77949836717
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10,12 and conversion of 4b to (S)-1b
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10,12 and conversion of 4b to (S)-1b.
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32
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77949835232
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Side-product formation led to diminished yields of the desired 4a
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Side-product formation led to diminished yields of the desired 4a.
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